U.S. patent number 7,435,238 [Application Number 11/005,327] was granted by the patent office on 2008-10-14 for needle device having retractable needle providing enhanced safety.
Invention is credited to Alan Reid.
United States Patent |
7,435,238 |
Reid |
October 14, 2008 |
Needle device having retractable needle providing enhanced
safety
Abstract
A medical device includes a base member coupled to a needle
assembly and a retractor mechanism enables retraction of the needle
into the base member for safe disposal of the device. In one
embodiment, a stop mechanism prevents rotation of the needle
assembly in a use position.
Inventors: |
Reid; Alan (Keene, NH) |
Family
ID: |
46303446 |
Appl.
No.: |
11/005,327 |
Filed: |
December 6, 2004 |
Prior Publication Data
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Document
Identifier |
Publication Date |
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US 20050080386 A1 |
Apr 14, 2005 |
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Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
Issue Date |
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10712600 |
Nov 13, 2003 |
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10242976 |
Sep 13, 2002 |
6755805 |
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Current U.S.
Class: |
604/192;
604/110 |
Current CPC
Class: |
A61M
5/158 (20130101); A61M 25/0612 (20130101); A61M
5/3243 (20130101); A61M 5/3275 (20130101); A61M
2005/1581 (20130101); A61M 2005/1583 (20130101) |
Current International
Class: |
A61M
5/32 (20060101); A61M 5/00 (20060101) |
Field of
Search: |
;604/110,188,192-198,164.08 |
References Cited
[Referenced By]
U.S. Patent Documents
Other References
Millenium Medical, Huber Plus Safety Infusion Set, Jan. 2000, 1
Page, Chadds Ford, Pennsylvania. cited by other.
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Primary Examiner: Sirmons; Kevin C.
Assistant Examiner: MacNeill; Elizabeth R
Attorney, Agent or Firm: Daly, Crowley, Mofford &
Durkee, LLP
Parent Case Text
CROSS REFERENCE TO RELATED APPLICATIONS
The present application is a continuation-in-part of U.S. patent
application Ser. No. 10/712,600, filed on Nov. 13, 2003, which is a
continuation-in-part of U.S. patent application Ser. No.
10/242,976, filed Sep. 13, 2002, now U.S. Pat. No. 6,755,805 which
is hereby incorporated by reference.
Claims
What is claimed is:
1. A medical device, comprising: a base member having first and
second ends, a longitudinal axis, and a channel extending along the
longitudinal axis; a needle assembly coupled to a first end of the
base member, the needle assembly including a needle extending from
an elongate member; a retractor mechanism coupled to the elongate
member enabling rotation of the needle and coupled to the base
member enabling retraction of a protruding needle in a use
position, in which the needle is unparallel to the longitudinal
axis, into the base member as the retractor mechanism slides in the
channel to a non-use position in which the needle is at least
partly captured in the base member, wherein retraction of the
protruding needle is produced by a first force on the base member
along the longitudinal axis and a second force on the retractor
mechanism that is counter to the first force; and at least one stop
mechanism to prevent rotation of the needle assembly with respect
to the base member, wherein the at least one stop mechanism
includes a protrusion on the elongate member that is insertable
into a corresponding aperture in the retractor mechanism to prevent
rotation of the needle.
2. The device according to claim 1, wherein in the use position the
needle is substantially orthogonal to the axis.
3. The device according to claim 1, wherein the at least one stop
mechanism is actuated by pressure from a user.
4. The device according to claim 3, wherein the at least one stop
mechanism is biased to the non-actuated position.
5. The device according to claim 1, wherein the retractor mechanism
includes at least one wing to receive pressure from a user.
6. The device according to claim 5, wherein the pressure on the at
least one wing and counter pressure on the first end of the base
member is effective to retract the needle assembly into the base
member.
7. A medical device, comprising: a base member having first and
second ends and a channel extending along an axis; a needle
assembly having a needle extending from an elongate member coupled
to the base member; and a retractor mechanism having first and
second prongs rotatably coupled to the elongate member of the
needle assembly and wings slidably coupled in the channel of the
base member to enable retraction of the needle from a use position
having the needle unparallel to the axis into the base member to a
non-use position having the needle substantially parallel to the
axis.
8. The device according to claim 7, further including a stop
mechanism to prevent rotation of the needle assembly.
9. The device according to claim 8, wherein the stop mechanism
includes a protrusion from the elongate member and a corresponding
aperture in the first prong of the retractor mechanism.
10. The device according to claim 7, wherein pressure against the
wings of the retractor mechanism and counter pressure against the
first end of the base member is effective to retract the needle
into the base member.
11. A method of fabricating a medical device, comprising: coupling
an elongate member of a needle assembly having a needle to a
retractor mechanism slidably coupled to a base member extending
along an axis having first and second ends such that pressure on
wings of the retractor mechanism and counter pressure on the first
end of the base member is effective to retract the needle into the
base member from a use position having the needle unparallel to the
axis to a non-use position having the needle substantially parallel
to the axis, wherein the wings of the retractor mechanism extend
through channels on either side of the base member.
12. The method according to claim 11, wherein the elongate member
includes a stop to prevent rotation of the needle.
Description
STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH
Not Applicable.
FIELD OF THE INVENTION
The present invention relates generally to medical devices and,
more particularly, to medical devices having a needle for insertion
into a patient.
BACKGROUND OF THE INVENTION
Medical devices for injecting fluids into a patient are well known
in the art. One such type of device is generally referred to as
implanted ports, which can be implanted subcutaneously in a
patient. Various types of ports can be used to provide access to
the peritoneal cavity, as well as the vascular, arterial, and
epidural systems. The ports typically include a catheter for access
to a large vein and a port body having a septum, which is generally
formed from silicone.
The port is implanted within a cavity formed in the patient, such
as in the chest area, and sutured to underlying tissue. From time
to time, it is desirable to refill the port via the septum and/or
provide an external source of fluid, e.g., IV access. One type of
device used to refill an implanted port is generally known as a
Huber needle. Known Huber needles generally include a needle
extending from a base structure. With sufficient expertise and
experience an operator, such as a nurse, can insert the needle into
the port via the septum, which is sliced (not cored) by the needle
for self-sealing. The Huber needle can then be taped to the patient
and fluid delivered to the patient intravenously as desired via a
coupled to the Huber needle device.
However, conventional Huber device can be relatively difficult to
remove from the patient. An operator may need to apply a
significant amount of force to initiate removal of the device. If
the needle suddenly releases, the operator may be accidentally
injured by the needle as it is uncontrollably freed from the
patient. In addition, even after safe removal, known Huber needle
devices can present a hazard due to the outwardly extending
needle.
It would, therefore, be desirable to overcome the aforesaid and
other disadvantages.
SUMMARY OF THE INVENTION
The present invention provides a medical device, such as a Huber
needle, having a needle and a structure that enhances user safety
during removal of the needle from a patient. The inventive
structure reduces the likelihood that medical personnel will suffer
injury from the needle as it is forcibly removed from the patient.
While the invention is primarily shown and described in conjunction
with a Huber-type needle, it is understood that the invention is
applicable to devices in general in which it is desirable to reduce
the possibility of injury from a needle.
In one aspect of the invention, a medical device includes a central
structural member from which a needle extends. At least one wing
portion extends from the central structural member for facilitating
removal of the needle from the patient in a controlled manner. A
base member for contacting the patient's skin is coupled to the
central structural member. First and second members are pivotably
secured to the base member so as to provide a structure that can be
transitioned from a use position in which the needle extends from
the device for insertion into the patient and a non-use position in
which the needle is captured by the first member as the needle is
extracted from the patient.
With this arrangement, an operator leverages pressure applied to
the wing portion(s) with a finger (s) and counter pressure on the
first member so as to enable a controlled removal of the needle
from the patient. In addition, the collapsible/expandable structure
captures the needle in the first member as it is removed from the
patient to enhance operator safety.
In another aspect of the invention, a medical device has a use
position and a non-use position with a housing having first and
second portions each having respective first and second ends. The
second portion has a first position in the use position and a
second position in the non-use position. A longitudinal member has
first and second ends and extends from the housing in the use
position. In the non-use position, the longitudinal member is
captured by the first housing portion. A needle extends from the
device in the use position and envelops the device the non-use
position. The device can include one or more locking mechanisms to
secure the device in the non-use position.
In a further aspect of the invention, a medical device has a use
position in which a needle is extended from a base member and a
non-use position in which the needle is captured in the base
member. A needle assembly having a needle is rotatably coupled to a
retractor mechanism to enable the needle to be retracted into the
base member to the non-use position. The medical device can include
a stop mechanism to prevent rotation of the needle.
BRIEF DESCRIPTION OF THE DRAWINGS
The invention will be more fully understood from the following
detailed description taken in conjunction with the accompanying
drawings, in which:
FIGS. 1A and 1B are perspective schematic depictions of a medical
device having enhanced safety in accordance with the present
invention in the non-use position;
FIG. 2A is a perspective schematic depiction of the medical device
of FIG. 1 in the non-use position;
FIG. 2B is a perspective schematic depiction of the medical device
of FIG. 2A in a use position;
FIG. 2C is a bottom perspective view of the device of FIG. 2B;
FIG. 3A is a perspective schematic depiction of a medical device
having enhanced safety in accordance with the present invention in
a non-use position;
FIG. 3B is a perspective schematic depiction of the medical device
of FIG. 3A in the use position;
FIG. 4A is a perspective schematic depiction of an exemplary
medical device having enhanced safety in accordance with the
present invention shown in a non-use position;
FIG. 4B is a top view of the device of FIG. 4A;
FIG. 4C is a sectional view of the device of FIG. 4B;
FIG. 5A is a top view of the exemplary medical device of FIG. 4A
shown in a use position; and
FIG. 5B is a sectional view of the device of FIG. 5A along line
5B.
FIG. 6 is a perspective schematic representation of an exemplary
medical device shown in a use position in accordance with the
present invention;
FIG. 7A is a top view of the medical device of FIG. 6;
FIG. 7B is a side view of the medical device of FIG. 6;
FIG. 7C is a bottom view of the medical device of FIG. 6;
FIG. 7D is a cross-sectional view along line 7D of the medical
device of FIG. 7B;
FIG. 8A is a top view of the medical device of FIG. 6 in a non-use
position;
FIG. 8B is a side view of the medical device of FIG. 6 in a non-use
position; and
FIG. 8C is a front view of the medical device of FIG. 6 is a
non-use position.
FIG. 9 is a perspective view of a medical device having a rotating
and retracting needle shown in a use position;
FIG. 10A is a top view of the medical device of FIG. 9;
FIG. 10B is a front view of the medical device of FIG. 9;
FIG. 10C is a side view of the medical device of FIG. 9
FIG. 11 is a perspective view of a medical device having a rotating
and retracting needle shown in a non-use position;
FIG. 12A is a top view of the medical device of FIG. 11;
FIG. 12B is a front view of the medical device of FIG. 11;
FIG. 12C is a side view of the medical device of FIG. 11; and
FIG. 13 is a perspective of a needle assembly and a retractor
mechanism that can form a part of the medical device of FIG. 9.
DETAILED DESCRIPTION OF THE INVENTION
FIGS. 1A-1B show a medical device 100 including a needle 102 and a
structure for enhanced operator safety in accordance with the
present invention. In general, the device structure facilitates
removal of the needle from a patient and captures the needle as it
is retracted from the patient's body. During use, the device is
relatively flat or collapsed and the needle extends outwardly for
insertion into an implanted port device, for example. After use,
the device is transitioned to the non-use position in which the
needle is captured within the device. As described below, the
device can include various features to prevent a transition to the
use position from the non-use position to preclude re-use of the
device.
The device 100 includes opposed first and second wing portions
104,a,b extending from a central structural member 106. As
described below, the wing portions 104 provide surfaces on which an
operator can apply pressure to insert the device. This arrangement
leverages the force applied to the device so as to provide smooth,
and safe, insertion and extraction of the needle from the
patient.
FIGS. 2A-2C show further details of an exemplary medical device
100' having a structure providing enhanced safety features in
accordance with the present invention. In general, the device of
FIGS. 1A and 1B is similar to the device of FIGS. 2A-2C in which
like reference designations indicate like elements. The device 100
includes a series of interconnected members that move with respect
to the central structural member 106 for safely transitioning the
device from use position to the non-use position. The various
members shown in FIGS. 2A and 2B are marked with a particular shape
as shown to designate the corresponding parts on each of these
figures.
A first member 110 is pivotably coupled to a skin-contacting base
member 108 at a pivot 112. In an exemplary embodiment, the first
member 110 includes an arcuate portion 110a for accommodating the
stacked members in the use position, as best shown in FIG. 2B. A
second member 114, at respective pivots 116, 118, extends between
the base member 108 and the first member 110. In one embodiment,
the second member 114 includes first and second sub portions 114a,b
joined at a pivot point 120 to enable the second member first and
second sub portions 114a,b to fold under the first member 110. It
is understood that these members have mirror images on each side of
the central structural member 106.
The device further includes a raised portion 122 that can form a
part of the first member 110. As shown in FIGS. 2A and 2B, the
raised portion 122 can include a depression 124 that can be
pressured by a operator's thumb, for example, to insert the device
into the patient. As used herein, the use position refers to the
needle outwardly extending from the device for insertion into a
patient. In the use position, the device is "flat" or
collapsed.
As shown in FIGS. 2B and 2C, (and 4C and 5B) for example, the
central structural member 106 can include a slotted channel 126
from which the needle extends perpendicularly, for example. The
needle 102 can have an L-shape to facilitate coupling of the needle
with a tube (not shown) disposed within the channel 126. The needle
can be secured within the channel 126 in a conventional manner,
such as by adhesive.
The device can include various features to improve the operation
and safety of the device. For example, the device can include one
or more latches to further enhance operator safety.
As shown in FIGS. 3A-3B, the device can include a first latching
mechanism 150 located at an end of the first member 110. In one
particular embodiment, the first latching mechanism includes a tab
152 to facilitate detachment of a latch member 150a from a
receiving aperture or cutout 150b in the central structural member
106. The latching mechanism 150 can be released to raise the first
member 110 by lifting the tab 152 prior to removal of the device
from the patient.
A second latch 180 shown in FIGS. 3A (and 4C) for example, can be
located at a tip of the first member 110 so that the needle is
retained within the first member. In an exemplary embodiment, the
needle 102 is captured by an arcuate cavity 182 formed in the first
member 110. Once the device transitions to the non-use position,
the second latch 180 prevents the device from transitioning to the
use position by retaining the needle within the cavity.
In another embodiment (not shown), the device can include
mechanisms to provide unidirectional movement to the non-use
position. In one embodiment, the first member includes a
ratchet-type device allowing only movement of the first member 110
away from the base member 108.
Referring again to FIGS. 2A-3B, the structure of the device 100
leverages the force applied to the wing portions 104 and the first
member 110 to ease extraction of the needle from the patient. In
one embodiment, while the device is flush with the patient's skin,
the operator moves the first member 110 to an upright position with
respect to the central structural member 106. The operator then
applies first and second fingers underneath the wing portions 104
and a thumb, for example, on or near the tab 152 of the first
member 110. By applying force on top of the upright first member
110, the implanted port is stabilized in position. The operator can
then apply force to lift the wing portions 104 up while applying a
counter-force on the first member 110 to leverage the force applied
on the wing portions.
The applied pressure forces the central structural member 106 and
wings 104 up and away from the base member 108 and the needle 102
retracts into the cavity 182 in first member 110. With this
arrangement, it is relatively easy for the operator to apply steady
pressure to the device for a smooth extraction of the needle from
the patient. That is, the needle is not suddenly freed from the
patient in a relatively out of control manner. It is understood
that the tab 152 can be shaped to facilitate movement of the first
member 110 to an upright position and to accommodate force applied
to the tab 152 by the operator's thumb.
FIGS. 4A-5B show further details of a Huber needle-type device,
such as the device 100 of FIGS. 1A and 1B, having enhanced safety
features in accordance with the present invention. FIGS. 4A-4C show
a device in the non-use position from a perspective, top, and
sectional view, respectively. FIG. 5A is a top view of a device in
the use position in accordance with the present invention and FIG.
5B is a sectional view taken along line 5B of FIG. 5A.
In one embodiment, the devices can be delivered in the use
position. As described above, the devices can include various
features to prevent a transition from the use position to the
non-use position.
In a further aspect of the invention shown in FIG. 6, a medical
device 200, which is shown in a user position, includes a
longitudinal member 202 that slides into a housing 204. In an
exemplary embodiment, the device 200 locks in a non-use position
after removal of a needle 206 from a patient. In general, when the
device 200 is in the use position, a user can apply finger pressure
to first and second wing portions 208a,b and thumb pressure to an
end 202a of the longitudinal member to force retraction of the
needle 206 from the patient's body. When the longitudinal member
202 is captured by the housing 204, the needle 206 no longer
protrudes from the device 200 to enhance operator safety.
FIGS. 7A-8C show further details of the device 200 shown in FIG. 6.
FIGS. 7A-7D show the device 200 in a first or use position and
FIGS. 8A-8C show the device 200 in a second or non-use position. A
user or operator transitions the device 200 from the use position
to the non-use position as described in detail below.
As shown in FIGS. 7A-7D, in the use position the needle 206
protrudes from the device 200 for insertion into a patient. The
device 200 is relatively flat in the use position so that a bottom
surface 210 can rest on a patient while the needle 206 is disposed
beneath the skin. The extended longitudinal member 202 includes a
channel 212, which can be centered about a longitudinal axis 214 of
the device. The needle 206 extends through the channel, which
allows axial movement of the longitudinal member. The longitudinal
member 202 further includes a first and optional second locking
mechanism 216a, 216b for securing the longitudinal member 202 in
the non-use position, as described more fully below.
In an exemplary embodiment, the housing 204 include first and
second portions 204a, 204b that are secured to each other. In one
embodiment, one end of the second housing portion 204b is coupled
to one end of the longitudinal member 202 and the other end of the
second housing portion is coupled to an end of the first housing
portion 204a. Optional first and second wing portions 208a, 208b
extend from the housing first portion 204a. The wing portions 208
can be arcuate as shown to receive, for example, the application of
force by the index and middle fingers of a user.
A needle retaining member 218 is disposed on the housing 204 for
securing the needle 206, which extends through the channel 212, in
the longitudinal member 202. The arrangement of the channel 212 and
the needle retaining member 218 secures the needle in position
while not interfering with movement of the longitudinal member 202
during transition of the device from the use position to the
non-use position.
In one embodiment, the housing 204 further includes first and
second locking members 220a, 220b that mechanically communicate
with the first and second locking members 216a, 216b of the
longitudinal member 202. In general, upon complete insertion of the
longitudinal member 202 into the housing 204, the housing locking
members 220 align and interlock with the longitudinal member
locking members 216. In the non-use position, the longitudinal
member 202 cannot be removed from the housing 204 to prevent re-use
of the device and promote user safety.
FIGS. 8A-8C show the medical device 200 in the non-use position
with the longitudinal member 202 fully inserted into housing 204
and the locking members 216, 220 engaged. The second housing
portion 204b includes a first piece 222a, and a second piece 222b
that can pivot with respect to each other. In the non-use position,
the first and second pieces 222 form an angle of about ninety
degrees in one particular embodiment. The angled first and second
pieces 222 extend outwardly from the first housing portion 204a so
as to envelope the needle 206. That is, in the non-use position,
the needle 206 does not protrude from the device 200. A slot 224
(FIG. 7C) in the second housing portion 204a enables the first and
second pieces 222 to pivot unencumbered by the needle 206.
In one particular embodiment, the non-pivoting end of the first
piece 222a is coupled to the end 202a of the longitudinal member.
As force is applied to the longitudinal member 202 to force it into
the housing 204, movement of the longitudinal member 202 pivots the
first piece 222a with respect to the second piece 222b. The
non-pivoting end of the second piece 222b is coupled to an end of
the first housing portion 204a.
In an exemplary embodiment, the second housing portion 204b
includes a series of ribs to create friction as the device 200
transitions to the non-use position during extraction of the needle
206 from the patient. As force is applied to the longitudinal
member 202, the pivoting first and second pieces 222 push against
the patient to withdraw the needle 206.
It is understood that the device dimensions can vary to meet the
needs of a particular application. In one embodiment, the device
has a length of about 2.3 inches and a height of about 1.5 inch in
the non-use position. The device can have a width measure from ends
of the wing portions of about 2.1 inches.
The inventive medical device shown and described herein can be
fabricated from a variety of suitable materials well known to one
of ordinary skill in the art. Exemplary materials include plastic,
such as PVC, polyethylene, and the like.
In another aspect of the invention, a medical device includes a
base member coupled to a needle assembly having a needle and to a
retractor mechanism to retract the needle into the base member. A
locking mechanism can prevent rotation of the needle.
FIG. 9 shows a medical device 300 (in the use position) having an
elongate base member 302 having a first end 304 and a second end
306. First and second protrusions 308a,b can extend from either
side of the base member first end 304. A channel 310 extends along
each side of the base member 302. At the second end 306 of the base
member a needle assembly 312 is coupled. As described more fully
below, the needle assembly 312 includes a needle 314 that can be
rotated to and locked in a use position in which the protruding
needle can be inserted into a patient. The needle assembly 312 can
also be rotated and retracted into the base member 302 to enhance
safety in a non-use position. A retractor mechanism 316 is coupled
to the needle assembly 312 and the base member 302 to receive force
applied by a user that is effective in combination with a counter
force applied to the first end of the base member 304 to retract
the needle 314 into the base member.
FIGS. 10A-C shows the medical device 300 of FIG. 9 in a top, front
and side view respectively, in the use position. In the use
position, the needle 314 extends generally perpendicularly from the
base member forming an "L" shape. In an exemplary embodiment, the
needle forms an angle in the range from about plus/minus ten
degrees with respect to the base member.
FIG. 11 shows the device 300 in the non-use position with the
needle 314 retracted and fully captured in the base member 302. The
needle 314 has been rotated about ninety degrees from the use
position (to form an angle of about 180 degrees) and then retracted
by moving the needle assembly 312 up the channel 310 towards the
first end 304 of the base member. In an exemplary embodiment, the
needle assembly 312 is secured in the non-use position to prevent
the needle 314 from exiting the base member after use.
FIGS. 12A-C show the device 300 in the top, front, and side view,
respectively in the non-use position. In one embodiment, the needle
314 is retracted until it is fully captured in the base member 302
so that the device can be safely disposed of after use.
FIG. 13 shows the needle assembly 312 and retractor mechanism 316
without the base member to more clearly show operation of the
device and to show a locking mechanism to secure the needle in
position as the needle is inserted into and/or removed from a
patient. The needle assembly 312 includes an elongate member 318,
which is shown as generally cylindrical, passing through apertures
320a,b in respective first and second prongs 322a,b of the
retractor mechanism 316. Each of the apertures 320 includes a
geometry having a first region 324 with an annular shape
complementing the cylindrical elongate member 318 and a second
region 326 having a geometry complementing respective stops 328a,b
on the elongate member 318. Tubing can be coupled to an end of the
elongate member 318 to provide a connection between an external
fluid source, e.g., medication, and the needle 314.
In the unlocked position, even where the stops 328 are aligned with
the apertures 320, the elongate member 318 and needle 314 can
rotate with respect to the retractor mechanism 316. In the use
position, the locked position can be achieved when a user pressures
the prongs 322 of the retractor mechanism together so that the
stops 328 are captured by the second regions 326 of the prongs.
While the stops are captured in the apertures 320, the needle
assembly is prevented from rotating to facilitate
insertion/extraction of the needle into a patient. In an exemplary
embodiment, the prongs 326 have a structural bias away from the
prongs 322 so that the unlocked position is the natural state of
the device.
The elongate member 318 can include optional protrusions 330
proximate ends of the elongate member to prevent the prongs 322
from sliding off the ends of the elongate member. Various other
mechanisms to provide the functionality of the protrusions will be
readily apparent to one of ordinary skill in the art.
While stops 328 and corresponding apertures 320 are shown to
prevent rotation of the needle, it is understood that a variety of
suitable alternative locking/stop mechanisms will be readily
apparent to one of ordinary skill in the art, such as ratchet
mechanisms, detent mechanism, and the like.
Referring now to FIGS. 9 and 11, from the use position, the needle
assembly 312 can be rotated ninety degrees while in the unlocked
position so that the needle 314 and base member 302 are aligned.
That is, the needle 314 and the base member are aligned linearly to
form an angle of about 180 degrees.
The user then applies pressure to the first end 304 of the base
member and counter pressure to wings 332 of the retractor mechanism
316 to move the elongate member 318 up the channel to the non-use
position. The user can then safely dispose of the device with the
needle 314 captured in the base member 302.
In one particular embodiment, the needle 314 is about one inch in
length NL. However, the length of the needle can vary to meet the
needs of a particular embodiment without departing from the
invention. The base member 302 is about two inches in length BL and
about one half inch in width BW in an exemplary embodiment but
these dimensions also can vary for a particular embodiment. From
tip to tip, the wings of the retractor mechanism can extend about
1.5 inches across AW in one particular embodiment. The distance DW
from the second end 306 of the base to the wings 332 is about 3/4
of an inch in one embodiment. And in the illustrated embodiment, a
distance WL from a side of the base 320 to a tip of the wing is
about one-half inch.
One skilled in the art will appreciate further features and
advantages of the invention based on the above-described
embodiments. Accordingly, the invention is not to be limited by
what has been particularly shown and described, except as indicated
by the appended claims. All publications and references cited
herein are expressly incorporated herein by reference in their
entirety.
* * * * *